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In order to further encourage and guide scientific and reasonable research on human bioavailability and bioequivalence of innovative drugs, our center has organized and drafted the "Technical Guidelines for Innovative Drugs on Human Bioavailability and Bioequivalence Research (Draft for Comment)", Now the center website is publicized to listen to opinions and suggestions from all walks of life.
The time limit for soliciting opinions is one month from the date of publication
Please send your feedback to the mailbox of the following contact:
Contact: Zhou Yu, Zhang Xuehui
Contact: zhouy@cde.
Thank you for your participation and great support
attachment1 : | "Guiding Principles for Research on Human Bioavailability and Bioequivalence of Innovative Drugs (Draft for Comment)". |
Annex 2: | "Guiding Principles for Research on Human Bioavailability and Bioequivalence of Innovative Drugs (Draft for Comment)" Drafting Instructions. |
Annex 3 : | Feedback form for soliciting opinions. docx |
Attachment 1:
"Technical Guidelines for Research on Human Bioavailability and Bioequivalence of Innovative Drugs (Draft for Comment)".
Appendix 2:
"Technical Guidelines for Research on Human Bioavailability and Bioequivalence of Innovative Drugs (Draft for Comment) )" Drafting Instructions.
Annex 3:
Feedback Form for Solicitation of Comments.
docx
Annex 1:
"Technical Guidelines for Research on Innovative Drugs on Human Bioavailability and Bioequivalence (Draft for Comment)".
Annex 1:
"Innovative Drugs on Human Biology" Technical Guidelines for Utilization and Bioequivalence Research (Draft for Comment)".
" Technical Guidelines for Research on Bioavailability and Bioequivalence of Innovative Drugs in Human Body (Draft for Comment)".
Annex 2:
"Innovative Drugs for Human Body Drafting Instructions for Technical Guiding Principles for Research on Bioavailability and Bioequivalence (Draft for Comment).
Annex 2:
Drafting instructions for Technical Guidelines for Research on Bioavailability and Bioequivalence of Innovative Drugs (Draft for Comment).
Drafting instructions for "Technical Guidelines for Research on Human Bioavailability and Bioequivalence of Innovative Drugs (Draft for Comment)".
Annex 3:
Feedback form for soliciting opinions.
docx
Annex 3:
Feedback form for soliciting opinions.
docx
Feedback form for soliciting opinions.
docx
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